scholarly journals Field metabolic rates of giant pandas reveal energetic adaptations

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Wenlei Bi ◽  
Rong Hou ◽  
Jacob R. Owens ◽  
James R. Spotila ◽  
Marc Valitutto ◽  
...  

AbstractKnowledge of energy expenditure informs conservation managers for long term plans for endangered species health and habitat suitability. We measured field metabolic rate (FMR) of free-roaming giant pandas in large enclosures in a nature reserve using the doubly labeled water method. Giant pandas in zoo like enclosures had a similar FMR (14,182 kJ/day) to giant pandas in larger field enclosures (13,280 kJ/day). In winter, giant pandas raised their metabolic rates when living at − 2.4 °C (36,108 kJ/day) indicating that they were below their thermal neutral zone. The lower critical temperature for thermoregulation was about 8.0 °C and the upper critical temperature was about 28 °C. Giant panda FMRs were somewhat lower than active metabolic rates of sloth bears, lower than FMRs of grizzly bears and polar bears and 69 and 81% of predicted values based on a regression of FMR versus body mass of mammals. That is probably due to their lower levels of activity since other bears actively forage for food over a larger home range and pandas often sit in a patch of bamboo and eat bamboo for hours at a time. The low metabolic rates of giant pandas in summer, their inability to acquire fat stores to hibernate in winter, and their ability to raise their metabolic rate to thermoregulate in winter are energetic adaptations related to eating a diet composed almost exclusively of bamboo. Differences in FMR of giant pandas between our study and previous studies (one similar and one lower) appear to be due to differences in activity of the giant pandas in those studies.

2004 ◽  
Vol 97 (5) ◽  
pp. 1915-1922 ◽  
Author(s):  
Wayne A. Van Voorhies ◽  
Aziz A. Khazaeli ◽  
James W. Curtsinger

In a recent study examining the relationship between longevity and metabolism in a large number of recombinant inbred Drosophila melanogaster lines, we found no indication of the inverse relationship between longevity and metabolic rate that one would expect under the classical “rate of living” model. A potential limitation in generalizing from that study is that it was conducted on experimental material derived from a single set of parental strains originally developed over 20 years ago. To determine whether the observations made with those lines are characteristic of the species, we studied metabolic rates and longevities in a second, independently derived set of recombinant inbred lines. We found no correlation in these lines between metabolic rate and longevity, indicating that the ability to both maintain a normal metabolic rate and have extended longevity may apply to D. melanogaster in general. To determine how closely our measurements reflect metabolic rates of flies maintained under conditions of life span assays, we used long-term, flow-through metabolic rate measurements and closed system respirometry to examine the effects of variables such as time of day, feeding state, fly density, mobility of the flies, and nitrogen knockout on D. melanogaster metabolic rate. We found that CO2 production estimated in individual flies accurately reflects metabolic rates of flies under the conditions used for longevity assays.


2021 ◽  
Author(s):  
◽  
Carla Edworthy

Ocean acidification (OA) is a global phenomenon referring to a decrease in ocean pH and a perturbation of the seawater carbonate system due to ever-increasing atmospheric CO2 concentrations. In coastal environments, identifying the impacts of OA is complex due to the multiple contributors to pH variability by coastal processes, such as freshwater inflow, upwelling, hydrodynamic processes, and biological activity. The aim of this PhD study was to quantify the local processes occurring in a temperate coastal embayment, Algoa Bay in South Africa, that contribute to pH and carbonate chemistry variability over time (monthly and 24-hour) and space (~10 km) and examine how this variability impacts a local fish species, Diplodus capensis, also commonly known as ‘blacktail’. Algoa Bay, known for its complex oceanography, is an interesting location in which to quantify carbonate chemistry variability. To assess this variability, monitoring sites were selected to coincide with the Algoa Bay Sentinel Site long-term ecological research (LTER) and continuous monitoring (CMP) programmes. The average pH at offshore sites in the bay was 8.03 ± 0.07 and at inshore sites was 8.04 ± 0.15. High pH variability (~0.55–0.61 pH units) was recorded at both offshore (>10 m depth) and inshore sites (intertidal surf zones). Many sites in the bay, especially the atypical site at Cape Recife, exhibit higher than the average pH levels (>8.04), suggesting that pH variability may be biologically driven. This is further evidenced by high diurnal variability in pH (~0.55 pH units). Although the specific drivers of the high pH variability in Algoa Bay could not be identified, baseline carbonate chemistry conditions were identified, which is necessary information to design and interpret biological experiments. Long-term, continuous monitoring is required to improve understanding of the drivers of pH variability in understudied coastal regions, like Algoa Bay. A local fisheries species, D. capensis, was selected as a model species to assess the impacts of future OA scenarios in Algoa Bay. It was hypothesized that this temperate, coastally distributed species would be adapted to naturally variable pH conditions and thus show some tolerance to low pH, considering that they are exposed to minimum pH levels of 7.77 and fluctuations of up to 0.55 pH units. Laboratory perturbation experiments were used to expose early postflexion stage of D. capensis to a range of pH treatments that were selected based on the measured local variability (~8.0–7.7 pH), as well as future projected OA scenarios (7.6–7.2 pH). Physiological responses were estimated using intermittent flow respirometry by quantifying routine and active metabolic rates as well as relative aerobic scope at each pH treatment. The behavioural responses of the larvae were also assessed at each pH treatment, as activity levels, by measuring swimming distance and speed in video-recording experiments, as well as feeding rates. D. capensis had sufficient physiological capacity to maintain metabolic performance at pH levels as low as 7.27, as evidenced by no changes in any of the measured metabolic rates (routine metabolic rate, active metabolic rate, and relative aerobic scope) after exposure to the range of pH treatments (8.02–7.27). Feeding rates of D. capensis were similarly unaffected by pH treatment. However, it appears that subtle increases in activity level (measured by swimming distance and swimming speed experiments) occur with a decrease in pH. These changes in activity level were a consequence of a change in behaviour rather than metabolic constraints. This study concludes, however, that based on the parameters measured, there is no evidence for survival or fitness related consequences of near future OA on D. capensis. OA research is still in its infancy in South Africa, and the potential impacts of OA to local marine resources has not yet been considered in local policy and resource management strategies. Integrating field monitoring and laboratory perturbation experiments is emerging as best practice in OA research. This is the first known study on the temperate south coast of South Africa to quantify local pH variability and to use this information to evaluate the biological response of a local species using relevant local OA scenarios as treatment levels for current and near future conditions. Research on local conditions in situ and the potential impacts of future OA scenarios on socio-economically valuable species, following the model developed in this study, is necessary to provide national policy makers with relevant scientific data to inform climate change management policies for local resources.


2020 ◽  
Vol 158 (5) ◽  
pp. 431-437
Author(s):  
Michael Kam ◽  
Shaher El-Meccawi ◽  
Arieh Brosh ◽  
A. Allan Degen

AbstractSheep are grazers and goats are intermediate feeders. By employing O2 consumption and heart rate measurements, resting metabolic rate (RMR) and field metabolic rate (FMR) were determined in four male fat-tailed Awassi sheep (44.0 ± 3.94) and four male Baladi goats (35.5 ± 5.42 kg) that were co-grazing natural pasture in the Negev Desert. There were 67.7 ± 3.75 g DM/m2 of herbaceous vegetation biomass, which was rapidly becoming senescent and more fibrous. We hypothesized that FMR of these desert-adapted ruminants would be relatively low when compared to other sheep and goat breeds, as animals in arid areas tend to have low metabolic rates. Both sheep (n = 6) and goats (n = 6) foraged 71% of the allotted 11 h free-pasture period; however, sheep grazed more than goats (P < 0.001); whereas goats browsed more than sheep (P < 0.001). RMR was higher (P = 0.007) in sheep than in goats (529 ± 23.5 v. 474 ± 25.4 kJ/kg0.75 BW/d), but FMR did not differ between species (618 ± 55.7 v. 613 ± 115.2 kJ/kg0.75 BW/d). In addition, the cost of activities, as a proportion of FMR, did not differ between sheep and goats; FMR increased by 89 kJ/kg0.75 BW/d or 17% in sheep and by 138 kJ/kg0.75 BW/d or 29% in goats. In comparing FMRs of sheep and goats in this study with these species in other studies, differences were inconsistent and, therefore, our hypothesis was not supported.


1997 ◽  
Vol 75 (11) ◽  
pp. 1781-1789 ◽  
Author(s):  
Patrice Boily ◽  
David M. Lavigne

Resting metabolic rate (RMR) data obtained from five juvenile and three adult female grey seals (Halichoerus grypus) in captivity over a period of 3.5 years were examined for developmental and seasonal changes. Three juveniles exhibited a significant relationship between log10 RMR and log10 mass, with individual slopes ranging from 0.42 to 1.62. Two of these exhibited a significant relationship between log10 RMR and log10 age. The remaining two juveniles and the three adults exhibited no significant relationship between RMR and body mass. With increasing size and age, RMRs of juveniles approached predicted values for adult mammals, but the large variation made it difficult to establish the precise age at which they achieved an adult-like RMR. RMRs of adults and juveniles exhibited marked seasonal changes. In juveniles, seasonal changes in RMR were limited to the annual moult, when the average RMR was 35% higher than during the rest of the year. In adults, changes in RMR were not limited to the time of the annual moult; rather, RMR was lower (by up to 50%) in the summer than during other seasons.


1988 ◽  
Vol 36 (3) ◽  
pp. 293 ◽  
Author(s):  
KA Nagy ◽  
AK Lee ◽  
RW Martin ◽  
MR Fleming

Field metabolic rates (FMRs) and rates of water flux in free-ranging fat-tailed dunnarts, Sminthopsis crassicaudata, were measured during spring (late October) using doubly labelled water. Feeding rates were estimated on the basis of water and energy fluxes. FMRs averaged 68.7 kJ d-' in adults (mean body mass= 16.6 g), and were 29.2 kJ d-' in juveniles (6.1 g). These FMRs are 6.6 times basal metabolic rate (BMR), and are much higher than the hypothetical maxima of four to five times BMR. Other dasyurid marsupials also have high FMR/BMR ratios, but so does a small petaurid marsupial. S. crassicaudata consumed 80-90% of its body mass in arthropods each day. The diet of arthropods apparently provided enough water for the animals to maintain water balance without drinking during this study.


2002 ◽  
Vol 205 (22) ◽  
pp. 3571-3575 ◽  
Author(s):  
Avner Anava ◽  
Michael Kam ◽  
Amiram Shkolnik ◽  
A. Allan Degen

SUMMARY Arabian babblers (Turdoides squamiceps; mean adult body mass=72.5 g) inhabit extreme deserts of Israel. Previous studies have shown that their daily field metabolic rates are similar in winter and summer and that there is an increase during the breeding season. We hypothesized that the difference in seasonal daily field metabolic rate would be a consequence of differences in daytime metabolic rate, and that night-time metabolic rate would be similar during the three seasons. We used doubly labelled water to determine daily,daytime and night-time field metabolic and water-influx rates in breeding babblers in spring and nonbreeding babblers in winter and summer. Daily and daytime energy expenditure rates were higher during the breeding season than during either summer or winter, but there was no difference among seasons in night-time energy expenditure rates. Thus, our hypothesis was supported. The daytime field metabolic rates in summer and winter nonbreeding babblers were 3.92× and 4.32× the resting metabolic rate (RMR),respectively, and in breeding babblers was 5.04× RMR, whereas the night-time field metabolic rates ranged between 1.26× RMR and 1.35× RMR in the three seasons. Daily and daytime water-influx rates were highest in winter, intermediate during the breeding season and lowest in summer, but there was no difference among seasons in night-time water-influx rate. Daytime water-influx rate was greater than night-time water-influx rate by 2.5-fold in summer, 3.9-fold in the breeding season and 6.75-fold in winter. Seasonal patterns of daily and daytime energy expenditure were similar, as were seasonal patterns of daily and daytime water influx. Daily and daytime energy expenditure and water-influx rates differed among seasons whereas night-time rates of both did not. Daily and daytime field metabolic rates of babblers were highest during the breeding season, whereas daily and daytime water-influx rates were highest in winter.


1989 ◽  
Vol 67 (3) ◽  
pp. 651-657 ◽  
Author(s):  
Robert A. MacArthur

Metabolic rates and body temperatures (Tb) of adult and immature beavers were recorded at air temperatures from −20 to 28 °C. The thermoneutral zone of beavers > 1 year of age extended from 0–2 °C to at least 28 °C. Lower critical temperature, whole-body conductance, and resting metabolic rate were similar for yearlings and beavers ≥ 2 years old, and conformed closely to weight-predicted values for terrestrial eutherians. The estimated lower critical temperature of a growing beaver kit declined from 24–25 °C at 2–3 weeks of age when the animal weighed 0.59–0.62 kg to 0–2 °C at 11–13 weeks when the kit weighed 2.92–3.50 kg. Rectal Tb of the kit was generally lower and less stable than abdominal Tb recorded telemetrically from older animals. In beavers > 1 year old, abdominal Tb was independent of air temprature (−20 to 28 °C), with no evidence of hypothermia or metabolic depression at subfreezing temperatures. Neither the level nor the daily rhythm of Tb was substantially altered by 24–48 h fasting in this species.


1985 ◽  
Vol 33 (5) ◽  
pp. 655 ◽  
Author(s):  
KA Nagy ◽  
RW Martin

Doubly labelled water measurements in free-ranging adult koalas (9.2 kg) indicated that field metabolic rates averaged 0.434 ml CO2 g-�h-� (equivalent to 2090 kJ per animal per day, or 2.59 X basal metabolic rate). Females (7.8 kg) had significantly higher mass-specific metabolic rates than males (10.8 kg). Percentage apparent assimilation of dietary substances was 56% for dry matter, 52% for energy, 32% for nitrogen, and 66% for water. Feeding rates were about 222 g dry food per animal per day (equivalent to 510 g fresh food per animal per day) in both sexes. However, males had a higher water influx rate (475 ml per animal per day) than females (358 ml per animal per day), suggesting either that males selected more succulent food than females, or that males drank rainwater but females did not. Koalas consumed about twice as much dietary nitrogen as they required for maintenance. They maintained constant body masses, and (presumably) had balanced energy, water and nitrogen budgets during our 20-day study, while eating Eucalyptus ovata foliage. Koalas spent about 4.7 h eating, 4 min travelling, 4.8 h resting while awake and 14.5 h sleeping in a 24-h period. Their activity periods were not obviously restricted to periods of daylight or darkness, but were scattered through the 24 hours. In comparison with free-living, three-toed sloths Bradypus variegatus (4.08 kg) in central America, koalas had significantly higher mass-corrected field metabolic rates (391 kJ kg-0.75 day-� for koalas v.209 for sloths), water influx rates (69.9 ml kg-0.80 day-� for koalas v. 49.8 for sloths), and feeding rates (42.7 g dry food kg-0.75 day-� for koalas v. 21.2 for sloths). Unlike sloths, koalas did not bask in the morning sunshine, and one telemetered koala had a relatively constant body temperature over 24 h (c. 36�C), compared with daily variations between 30 and 38�C in sloths. Population food consumption (g dry food consumed ha-� day-�) was greater for koalas (681 v. 378 for sloths), and koalas consumed most of the leaf production of their preferred food species, E. ovata, which resulted in extensive defoliation of these trees. Although there is similarity in the ecological roles of koalas and sloths, their physiology and behaviour differ substantially.


Author(s):  
Emma Moffett ◽  
David Fryxell ◽  
Kevin Simon

Acute exposure to warming temperatures increases minimum energetic requirements in ectotherms. However, over and within multiple generations, increased temperatures may cause plastic and evolved changes that modify the temperature sensitivity of energy demand and alter individual behaviours. Here, we aimed to test whether populations recently exposed to geothermally elevated temperatures express an altered temperature sensitivity of metabolism and behaviour. We expected that long-term exposure to warming would moderate metabolic rate, reducing the temperature sensitivity of metabolism, with concomitant reductions in boldness and activity. We compared the temperature sensitivity of metabolic rate (acclimation at 20 versus 30°C) and allometric slopes of routine, standard, and maximum metabolic rates, in addition to boldness and activity behaviours, across eight recently divergent populations of a widespread fish species (Gambusia affinis). Our data reveal that warm-source populations express a reduced temperature sensitivity of metabolism, with relatively high metabolic rates at cool acclimation temperatures and relatively low metabolic rates at warm acclimation temperatures. Allometric scaling of metabolism did not differ with thermal history. Across individuals from all populations combined, higher metabolic rates were associated with higher boldness and activity. However, warm-source populations displayed relatively more bold behaviour at both acclimation temperatures, despite their relatively low metabolic rates at warm acclimation temperatures. Overall, our data suggest that in response to warming, multigenerational processes may not direct trait change along a simple “pace-of-life syndrome” axis, instead causing relative decreases in metabolism and increases in boldness. Ultimately, our data suggest that multigenerational warming may produce a novel combination of physiological and behavioural traits, with consequences for animal performance in a warming world.


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